Issue 3, 2011

High resolution spectroscopy of methyltrioxorhenium: towards the observation of parity violation in chiral molecules

Abstract

Originating from the weak interaction, parity violation in chiral molecules has been considered as a possible origin of biohomochirality. We have proposed the observation of molecular parity violation using the two-photon Ramsey fringes technique on a supersonic beam. As a first step in this direction, a detailed spectroscopic study of methyltrioxorhenium (MTO) has been undertaken. It is an ideal test molecule as the achiral parent molecule of chiral candidates for a parity violation experiment. For the 187Re MTO isotopologue, a combined analysis of Fourier transform microwave and infrared spectra as well as ultra-high resolution CO2 laser absorption spectra enabled the assignment of 28 rotational lines and 71 rovibrational lines, some of them with a resolved hyperfine structure. A set of spectroscopic parameters in the ground and first excited state, including hyperfine structure constants, was obtained for the νas antisymmetric Re[double bond, length as m-dash]O stretching mode of this molecule. This result validates the experimental approach to be followed once a chiral derivative of MTO is synthesized, and shows the benefit of the combination of several spectroscopic techniques in different spectral regions, with different set-ups and resolutions. The first high resolution spectra of jet-cooled MTO, obtained on a set-up being developed for the observation of molecular parity violation, are shown, which constitutes a major step towards the targeted objective.

Graphical abstract: High resolution spectroscopy of methyltrioxorhenium: towards the observation of parity violation in chiral molecules

Supplementary files

Article information

Article type
Paper
Submitted
14 Sep 2010
Accepted
01 Nov 2010
First published
30 Nov 2010

Phys. Chem. Chem. Phys., 2011,13, 854-863

High resolution spectroscopy of methyltrioxorhenium: towards the observation of parity violation in chiral molecules

C. Stoeffler, B. Darquié, A. Shelkovnikov, C. Daussy, A. Amy-Klein, C. Chardonnet, L. Guy, J. Crassous, T. R. Huet, P. Soulard and P. Asselin, Phys. Chem. Chem. Phys., 2011, 13, 854 DOI: 10.1039/C0CP01806F

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